Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Analysis of methionine synthase (rs1805087) gene polymorphism in autism patients in Northern Iran.

Acta neurobiologiae experimentalis - 1 Jan 2016

Haghiri Rosa, Mashayekhi Farhad, Bidabadi Elham, Salehi Zivar

Abstract excerpt

Autism is characterized by impairment in reciprocal communication and speech, repetitive behaviors, and social communication. The genetic and environmental factors play roles in the pathogenesis of autism. It was recently shown that the genes involved in the folate/homocysteine pathway may be risk factors for autistic children. One of the genes that may be the risk factor for autism is Methionine synthase (MTR)....

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase
Share to Autistic Disorder

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Child, Preschool

Share to DNA Mutational Analysis

Share to Gene Frequency

Share to Risk Factors

Source

Identifiers

PMID: 28094822
DOI: 10.21307/ane-2017-030

Genes

MTR

Variants

rs1805087

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of methionine synthase (rs1805087) gene polymorphism in autism patients in Northern Iran.PMID 28094822Read ↗

<i>MTHFR</i> Gene C677T Polymorphism in Autism Spectrum DisordersSemantic proximity Read ↗

Methylenetetrahydrofolate reductase polymorphisms C677T and risk of autism in the Chinese Han population.Semantic proximity Read ↗

Study of the C677T and 1298AC polymorphic genotypes of MTHFR Gene in autism spectrum disorderSemantic proximity Read ↗

Association of methylenetetrahydrofolate reductase (MTHFR) gene C677T polymorphism with autism: evidence of genetic susceptibility.Semantic proximity Read ↗

Aberrations in folate metabolic pathway and altered susceptibility to autism.Semantic proximity Read ↗

Association between MTHFR gene polymorphisms and the risk of autism spectrum disorders: a meta-analysis.Semantic proximity Read ↗

Analysis of association between components of the folate metabolic pathway and autism spectrum disorder in eastern Indian subjects.Semantic proximity Read ↗

MTHFR C677T is not a risk factor for autism spectrum disorders in South Brazil.Semantic proximity Read ↗

Association Study of Polymorphisms in Genes Relevant to Vitamin B12 and Folate Metabolism with Childhood Autism Spectrum Disorder in a Han Chinese Population.Semantic proximity Read ↗

Association between MTHFR C677T/A1298C and susceptibility to autism spectrum disorders: a meta-analysis.Semantic proximity Read ↗

Clinical utility of folate pathway genetic polymorphisms in the diagnosis of autism spectrum disorders.Semantic proximity Read ↗

Genetic Susceptibility to Autism Spectrum Disorders: Folate Pathway Polymorphisms, Mediterranean Diet and Evolutionary Insights.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.